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人类癌症中的Fbxw7/hCdc4肿瘤抑制因子

The Fbxw7/hCdc4 tumor suppressor in human cancer.

作者信息

Tan YingMeei, Sangfelt Olle, Spruck Charles

机构信息

Department of Tumor Cell Biology, Sidney Kimmel Cancer Center, San Diego, CA 92121, USA.

出版信息

Cancer Lett. 2008 Nov 18;271(1):1-12. doi: 10.1016/j.canlet.2008.04.036. Epub 2008 Jun 9.

Abstract

Fbxw7/hCdc4 is a member of the F-box family of proteins, which function as interchangeable substrate recognition components of the SCF ubiquitin ligases. SCF(Fbxw7/hCdc4) targets several important oncoproteins including c-Myc, c-Jun, cyclin E1, and Notch, for ubiquitin-dependent proteolysis. Recent studies have shown that FBXW7/hCDC4 is mutated in a variety of human tumor types, suggesting that it is a general tumor suppressor in human cancer. Alteration of Fbxw7/hCdc4 function is linked to defects in differentiation, cellular proliferation, and genetic instability. In this review, we summarize what is known about Fbxw7/hCdc4-mediated degradation in the regulation of cellular proliferation and discuss how alteration of its function contributes to human tumorigenesis.

摘要

Fbxw7/hCdc4是F-box蛋白家族的成员,该家族作为SCF泛素连接酶可互换的底物识别成分发挥作用。SCF(Fbxw7/hCdc4)靶向包括c-Myc、c-Jun、细胞周期蛋白E1和Notch在内的几种重要的癌蛋白,进行泛素依赖性蛋白水解。最近的研究表明,FBXW7/hCDC4在多种人类肿瘤类型中发生突变,这表明它是人类癌症中的一种普遍的肿瘤抑制因子。Fbxw7/hCdc4功能的改变与分化缺陷、细胞增殖和基因不稳定有关。在这篇综述中,我们总结了关于Fbxw7/hCdc4介导的降解在细胞增殖调控中的已知信息,并讨论了其功能改变如何导致人类肿瘤发生。

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